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A new PEDV strain CH/HLJJS/2022 can challenge current detection methods and vaccines

BACKGROUND: Porcine epidemic diarrhea virus (PEDV) variant strains cause great economic losses to the global swine industry. However, vaccines do not provide sufficient protection against currently circulating strains due to viral mutations. This study traced the molecular characteristics of the mos...

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Autores principales: Yao, Xin, Qiao, Wen-Ting, Zhang, Yu-Qian, Lu, Wei-Hong, Wang, Zhen-Wei, Li, Hui-Xin, Li, Jin-Long
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859669/
https://www.ncbi.nlm.nih.gov/pubmed/36670408
http://dx.doi.org/10.1186/s12985-023-01961-z
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author Yao, Xin
Qiao, Wen-Ting
Zhang, Yu-Qian
Lu, Wei-Hong
Wang, Zhen-Wei
Li, Hui-Xin
Li, Jin-Long
author_facet Yao, Xin
Qiao, Wen-Ting
Zhang, Yu-Qian
Lu, Wei-Hong
Wang, Zhen-Wei
Li, Hui-Xin
Li, Jin-Long
author_sort Yao, Xin
collection PubMed
description BACKGROUND: Porcine epidemic diarrhea virus (PEDV) variant strains cause great economic losses to the global swine industry. However, vaccines do not provide sufficient protection against currently circulating strains due to viral mutations. This study traced the molecular characteristics of the most recent isolates in China and aimed to provide a basis for the prevention and treatment of PEDV. METHODS: We obtained samples from a Chinese diarrheal swine farm in 2022. Reverse transcription polymerase chain reaction and immunofluorescence were used to determine the etiology, and the full-length PEDV genome was sequenced. Nucleotide similarity was calculated using MEGA to construct a phylogenetic tree and DNASTAR. Mutant amino acids were aligned using DNAMAN and modeled by SWISS-MODEL, Phyre2 and FirstGlance in JMOL for protein tertiary structure simulation. Additionally, TMHMM was used for protein function prediction. RESULTS: A PEDV virulent strain CH/HLJJS/2022 was successfully isolated in China. A genome-wide based phylogenetic analysis suggests that it belongs to the GII subtype, and 96.1–98.9% homology existed in the whole genomes of other strains. For the first time, simultaneous mutations of four amino acids were found in the highly conserved membrane (M) and nucleocapsid (N) proteins, as well as eight amino acid mutations that differed from the vast majority of strains in the spike (S) protein. Three of the mutations alter the S-protein spatial structure. In addition, typing markers exist during strain evolution, but isolates are using the fusion of specific amino acids from multiple variant strains to add additional features, as also demonstrated by protein alignments and 3D models of numerous subtype strains. CONCLUSION: The newly isolated prevalent strain CH/HLJJS/2022 belonged to the GII subtype, and thirteen mutations different from other strains were found, including mutations in the highly conserved m and N proteins, and in the S1° and COE neutralizing epitopes of the S protein. PEDV is breaking through original cognitions and moving on a more complex path. Surveillance for PEDV now and in the future and improvements derived from mutant strain vaccines are highly warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-01961-z.
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spelling pubmed-98596692023-01-22 A new PEDV strain CH/HLJJS/2022 can challenge current detection methods and vaccines Yao, Xin Qiao, Wen-Ting Zhang, Yu-Qian Lu, Wei-Hong Wang, Zhen-Wei Li, Hui-Xin Li, Jin-Long Virol J Research BACKGROUND: Porcine epidemic diarrhea virus (PEDV) variant strains cause great economic losses to the global swine industry. However, vaccines do not provide sufficient protection against currently circulating strains due to viral mutations. This study traced the molecular characteristics of the most recent isolates in China and aimed to provide a basis for the prevention and treatment of PEDV. METHODS: We obtained samples from a Chinese diarrheal swine farm in 2022. Reverse transcription polymerase chain reaction and immunofluorescence were used to determine the etiology, and the full-length PEDV genome was sequenced. Nucleotide similarity was calculated using MEGA to construct a phylogenetic tree and DNASTAR. Mutant amino acids were aligned using DNAMAN and modeled by SWISS-MODEL, Phyre2 and FirstGlance in JMOL for protein tertiary structure simulation. Additionally, TMHMM was used for protein function prediction. RESULTS: A PEDV virulent strain CH/HLJJS/2022 was successfully isolated in China. A genome-wide based phylogenetic analysis suggests that it belongs to the GII subtype, and 96.1–98.9% homology existed in the whole genomes of other strains. For the first time, simultaneous mutations of four amino acids were found in the highly conserved membrane (M) and nucleocapsid (N) proteins, as well as eight amino acid mutations that differed from the vast majority of strains in the spike (S) protein. Three of the mutations alter the S-protein spatial structure. In addition, typing markers exist during strain evolution, but isolates are using the fusion of specific amino acids from multiple variant strains to add additional features, as also demonstrated by protein alignments and 3D models of numerous subtype strains. CONCLUSION: The newly isolated prevalent strain CH/HLJJS/2022 belonged to the GII subtype, and thirteen mutations different from other strains were found, including mutations in the highly conserved m and N proteins, and in the S1° and COE neutralizing epitopes of the S protein. PEDV is breaking through original cognitions and moving on a more complex path. Surveillance for PEDV now and in the future and improvements derived from mutant strain vaccines are highly warranted. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12985-023-01961-z. BioMed Central 2023-01-20 /pmc/articles/PMC9859669/ /pubmed/36670408 http://dx.doi.org/10.1186/s12985-023-01961-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yao, Xin
Qiao, Wen-Ting
Zhang, Yu-Qian
Lu, Wei-Hong
Wang, Zhen-Wei
Li, Hui-Xin
Li, Jin-Long
A new PEDV strain CH/HLJJS/2022 can challenge current detection methods and vaccines
title A new PEDV strain CH/HLJJS/2022 can challenge current detection methods and vaccines
title_full A new PEDV strain CH/HLJJS/2022 can challenge current detection methods and vaccines
title_fullStr A new PEDV strain CH/HLJJS/2022 can challenge current detection methods and vaccines
title_full_unstemmed A new PEDV strain CH/HLJJS/2022 can challenge current detection methods and vaccines
title_short A new PEDV strain CH/HLJJS/2022 can challenge current detection methods and vaccines
title_sort new pedv strain ch/hljjs/2022 can challenge current detection methods and vaccines
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9859669/
https://www.ncbi.nlm.nih.gov/pubmed/36670408
http://dx.doi.org/10.1186/s12985-023-01961-z
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